scholarly journals Angiotensin II Receptor Blockers Inhibit the Generation of Epoxyeicosatrienoic Acid from Arachidonic Acid in Recombinant CYP2C9, CYP2J2 and Human Liver Microsomes

2017 ◽  
Vol 121 (4) ◽  
pp. 239-245 ◽  
Author(s):  
Asuna Senda ◽  
Yuji Mukai ◽  
Toru Hayakawa ◽  
Yuka Kato ◽  
Erik Eliasson ◽  
...  
2015 ◽  
Vol 38 (12) ◽  
pp. 1975-1979 ◽  
Author(s):  
Asuna Senda ◽  
Yuji Mukai ◽  
Takaki Toda ◽  
Toru Hayakawa ◽  
Miki Yamashita ◽  
...  

2010 ◽  
Vol 6 (3) ◽  
pp. 33
Author(s):  
Robert J Petrella ◽  

It is widely recognised that hypertension is a major risk factor for the development of future cardiovascular (CV) events, which in turn are a major cause of morbidity and mortality. Blood pressure (BP) control with antihypertensive drugs has been shown to reduce the risk of CV events. Angiotensin-II receptor blockers (ARBs) are one such class of antihypertensive drugs and randomised controlled trials (RCTs) have shown ARB-based therapies to have effective BP-lowering properties. However, data obtained under these tightly controlled settings do not necessarily reflect actual experience in clinical practice. Real-life databases may offer alternative information that reflects an uncontrolled real-world setting and complements and expands on the findings of clinical trials. Recent analyses of practice-based real-life databases have shown ARB-based therapies to be associated with better persistence and adherence rates and with superior BP control than non-ARB-based therapies. Analyses of real-life databases also suggest that ARB-based therapies may be associated with a lower risk of CV events than other antihypertensive-drug-based therapies.


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